(E)-1-(Dimethylphenylsilyl)-1-buten-3-ol ((tert-butyldimethylsilyl)oxy)acetate | 133323-30-5

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: (E)-1-(Dimethylphenylsilyl)-1-buten-3-ol ((tert-butyldimethylsilyl)oxy)acetate
• 英文别名: (E)-1-(Dimethylphenylsilyl)-1-buten-3-ol [(tert-butyldimethylsilyl)oxy]acetate；[(E)-4-[dimethyl(phenyl)silyl]but-3-en-2-yl] 2-[tert-butyl(dimethyl)silyl]oxyacetate
• CAS: 133323-30-5
• 化学式: C₂₀H₃₄O₃Si₂
• 分子量: 378.659
• InChiKey: ONPYLQCIFJBYSZ-CCEZHUSRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.65
• 重原子数：
  25.0
• 可旋转键数：
  7.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  35.53
• 氢给体数：
  0.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  (E)-1-(Dimethylphenylsilyl)-1-buten-3-ol ((tert-butyldimethylsilyl)oxy)acetate 、 (E)-(2S,3R)-2-((tert-Butyldiphenylsilyl)oxy)-3-(dimethylphenylsilyl)-4-hexenoic acid 在 吡啶 、 三甲基氯硅烷 、 lithium diisopropyl amide 作用下， 生成 (E)-(2R^*,3R^*)-2-((tert-Butyldimethylsilyl)oxy)-3-(dimethylphenylsilyl)-4-hexenoic acid 、 (E)-(2S^*,3R^*)-2-((tert-Butyldimethylsilyl)oxy)-3-(dimethylphenylsilyl)-4-hexenoic acid
  参考文献：
  名称：

  Claisen rearrangements of enantiomerically pure C3-(acyloxy)-(E)-vinylsilanes

  摘要：

  The Ireland ester Claisen rearrangement of chiral (R)- and (S)-C3-(acyloxy)-(E)-vinylsilanes gives access to a wide range of alpha-chiral-beta-silyl-(E)-hexenoic acids with useful levels of diastereoselectivity for both the 2,3-syn and 2,3-anti diastereomers as illustrated in eqs 1 and 2. The vicinal diastereoselectivities for simple propionate esters rac-1b, (S)-1e, and (R)-1g can be varied from 1:12 to 16:1 (syn:anti) depending on reaction conditions. The employment of appropriately protected glycolate esters yields Claisen products with diastereoselectivities ranging from 23:1 (syn:anti), resulting from chelation control of enolate geometry, to 1:3.6 (syn:anti) via the use of a nonchelating, silicon-protecting group. The reaction of alpha-azido acetate (R)-1i is the first example of a Claisen rearrangement involving an alpha-azido ester and results in a new approach toward the asymmetric synthesis of alpha-amino acids. The assignment of relative stereochemistry based on the vicinal coupling constant data has been well documented.

  DOI：

  10.1021/jo00010a046
• 作为产物：
  描述：

  (E)-4-(dimethyl(phenyl)silyl)but-3-en-2-ol 、 2-[[(1,1-二甲基乙基)二甲基甲硅烷基]氧基]乙酸 在 4-二甲氨基吡啶 N,N'-二环己基碳二亚胺 作用下， 以 二氯甲烷 为溶剂， 以80%的产率得到(E)-1-(Dimethylphenylsilyl)-1-buten-3-ol ((tert-butyldimethylsilyl)oxy)acetate
  参考文献：
  名称：

  Claisen rearrangements of enantiomerically pure C3-(acyloxy)-(E)-vinylsilanes

  摘要：

  The Ireland ester Claisen rearrangement of chiral (R)- and (S)-C3-(acyloxy)-(E)-vinylsilanes gives access to a wide range of alpha-chiral-beta-silyl-(E)-hexenoic acids with useful levels of diastereoselectivity for both the 2,3-syn and 2,3-anti diastereomers as illustrated in eqs 1 and 2. The vicinal diastereoselectivities for simple propionate esters rac-1b, (S)-1e, and (R)-1g can be varied from 1:12 to 16:1 (syn:anti) depending on reaction conditions. The employment of appropriately protected glycolate esters yields Claisen products with diastereoselectivities ranging from 23:1 (syn:anti), resulting from chelation control of enolate geometry, to 1:3.6 (syn:anti) via the use of a nonchelating, silicon-protecting group. The reaction of alpha-azido acetate (R)-1i is the first example of a Claisen rearrangement involving an alpha-azido ester and results in a new approach toward the asymmetric synthesis of alpha-amino acids. The assignment of relative stereochemistry based on the vicinal coupling constant data has been well documented.

  DOI：

  10.1021/jo00010a046